GB679562A - Polymers and a process for the preparation thereof - Google Patents
Polymers and a process for the preparation thereofInfo
- Publication number
- GB679562A GB679562A GB29343/49A GB2934349A GB679562A GB 679562 A GB679562 A GB 679562A GB 29343/49 A GB29343/49 A GB 29343/49A GB 2934349 A GB2934349 A GB 2934349A GB 679562 A GB679562 A GB 679562A
- Authority
- GB
- United Kingdom
- Prior art keywords
- vinyl
- polymers
- allyl
- chloride
- methyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 229920000642 polymer Polymers 0.000 title abstract 13
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 abstract 5
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 abstract 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 4
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 abstract 4
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 abstract 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 abstract 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 abstract 3
- JLIDVCMBCGBIEY-UHFFFAOYSA-N 1-penten-3-one Chemical compound CCC(=O)C=C JLIDVCMBCGBIEY-UHFFFAOYSA-N 0.000 abstract 2
- JESXATFQYMPTNL-UHFFFAOYSA-N 2-ethenylphenol Chemical compound OC1=CC=CC=C1C=C JESXATFQYMPTNL-UHFFFAOYSA-N 0.000 abstract 2
- 206010001497 Agitation Diseases 0.000 abstract 2
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 abstract 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 abstract 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 abstract 2
- FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 abstract 2
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 abstract 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract 2
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Natural products OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 abstract 2
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 abstract 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 abstract 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 abstract 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 abstract 2
- 238000013019 agitation Methods 0.000 abstract 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 abstract 2
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 abstract 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 abstract 2
- 239000003701 inert diluent Substances 0.000 abstract 2
- 239000012442 inert solvent Substances 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 abstract 2
- -1 vinyl allyl phthalate Chemical compound 0.000 abstract 2
- 229920002554 vinyl polymer Polymers 0.000 abstract 2
- PMJHHCWVYXUKFD-SNAWJCMRSA-N (E)-1,3-pentadiene Chemical group C\C=C\C=C PMJHHCWVYXUKFD-SNAWJCMRSA-N 0.000 abstract 1
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 abstract 1
- UZKWTJUDCOPSNM-UHFFFAOYSA-N 1-ethenoxybutane Chemical compound CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 abstract 1
- OYLCUJRJCUXQBQ-UHFFFAOYSA-N 1-hepten-3-one Chemical compound CCCCC(=O)C=C OYLCUJRJCUXQBQ-UHFFFAOYSA-N 0.000 abstract 1
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 abstract 1
- IGGDKDTUCAWDAN-UHFFFAOYSA-N 1-vinylnaphthalene Chemical compound C1=CC=C2C(C=C)=CC=CC2=C1 IGGDKDTUCAWDAN-UHFFFAOYSA-N 0.000 abstract 1
- GBURUDXSBYGPBL-UHFFFAOYSA-N 2,2,3-trimethylhexanedioic acid Chemical compound OC(=O)C(C)(C)C(C)CCC(O)=O GBURUDXSBYGPBL-UHFFFAOYSA-N 0.000 abstract 1
- CISIJYCKDJSTMX-UHFFFAOYSA-N 2,2-dichloroethenylbenzene Chemical compound ClC(Cl)=CC1=CC=CC=C1 CISIJYCKDJSTMX-UHFFFAOYSA-N 0.000 abstract 1
- PIGJZPZYWKFDBR-UHFFFAOYSA-N 2,5-dimethyl-1-(4-methylpyridin-2-yl)pyrrole-3-carbaldehyde Chemical compound CC1=CC(C=O)=C(C)N1C1=CC(C)=CC=N1 PIGJZPZYWKFDBR-UHFFFAOYSA-N 0.000 abstract 1
- DGXAGETVRDOQFP-UHFFFAOYSA-N 2,6-dihydroxybenzaldehyde Chemical compound OC1=CC=CC(O)=C1C=O DGXAGETVRDOQFP-UHFFFAOYSA-N 0.000 abstract 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 abstract 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract 1
- FEUFEGJTJIHPOF-UHFFFAOYSA-N 2-butyl acrylic acid Chemical compound CCCCC(=C)C(O)=O FEUFEGJTJIHPOF-UHFFFAOYSA-N 0.000 abstract 1
- TVONJMOVBKMLOM-UHFFFAOYSA-N 2-methylidenebutanenitrile Chemical compound CCC(=C)C#N TVONJMOVBKMLOM-UHFFFAOYSA-N 0.000 abstract 1
- OHXAOPZTJOUYKM-UHFFFAOYSA-N 3-Chloro-2-methylpropene Chemical compound CC(=C)CCl OHXAOPZTJOUYKM-UHFFFAOYSA-N 0.000 abstract 1
- ZXABMDQSAABDMG-UHFFFAOYSA-N 3-ethenoxyprop-1-ene Chemical compound C=CCOC=C ZXABMDQSAABDMG-UHFFFAOYSA-N 0.000 abstract 1
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 abstract 1
- FKWUKKNHLHTXJE-UHFFFAOYSA-N 5-o-ethenyl 1-o-methyl pentanedioate Chemical compound COC(=O)CCCC(=O)OC=C FKWUKKNHLHTXJE-UHFFFAOYSA-N 0.000 abstract 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 abstract 1
- OSDWBNJEKMUWAV-UHFFFAOYSA-N Allyl chloride Chemical compound ClCC=C OSDWBNJEKMUWAV-UHFFFAOYSA-N 0.000 abstract 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 abstract 1
- 239000004641 Diallyl-phthalate Substances 0.000 abstract 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 abstract 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical group CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 abstract 1
- 229910002651 NO3 Inorganic materials 0.000 abstract 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 abstract 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 abstract 1
- 239000004952 Polyamide Substances 0.000 abstract 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 abstract 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 abstract 1
- 229920000180 alkyd Polymers 0.000 abstract 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 abstract 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 229940050390 benzoate Drugs 0.000 abstract 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 abstract 1
- AJCHRUXIDGEWDK-UHFFFAOYSA-N bis(ethenyl) butanedioate Chemical compound C=COC(=O)CCC(=O)OC=C AJCHRUXIDGEWDK-UHFFFAOYSA-N 0.000 abstract 1
- JZQAAQZDDMEFGZ-UHFFFAOYSA-N bis(ethenyl) hexanedioate Chemical compound C=COC(=O)CCCCC(=O)OC=C JZQAAQZDDMEFGZ-UHFFFAOYSA-N 0.000 abstract 1
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 abstract 1
- HABAXTXIECRCKH-UHFFFAOYSA-N bis(prop-2-enyl) butanedioate Chemical compound C=CCOC(=O)CCC(=O)OCC=C HABAXTXIECRCKH-UHFFFAOYSA-N 0.000 abstract 1
- FPODCVUTIPDRTE-UHFFFAOYSA-N bis(prop-2-enyl) hexanedioate Chemical compound C=CCOC(=O)CCCCC(=O)OCC=C FPODCVUTIPDRTE-UHFFFAOYSA-N 0.000 abstract 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 abstract 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 150000004651 carbonic acid esters Chemical class 0.000 abstract 1
- 229920002678 cellulose Polymers 0.000 abstract 1
- 239000001913 cellulose Substances 0.000 abstract 1
- 229920002301 cellulose acetate Polymers 0.000 abstract 1
- FOCAUTSVDIKZOP-UHFFFAOYSA-M chloroacetate Chemical compound [O-]C(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-M 0.000 abstract 1
- 229940089960 chloroacetate Drugs 0.000 abstract 1
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 abstract 1
- 239000011248 coating agent Substances 0.000 abstract 1
- 229920001577 copolymer Polymers 0.000 abstract 1
- IEPRKVQEAMIZSS-AATRIKPKSA-N diethyl fumarate Chemical compound CCOC(=O)\C=C\C(=O)OCC IEPRKVQEAMIZSS-AATRIKPKSA-N 0.000 abstract 1
- 150000002009 diols Chemical class 0.000 abstract 1
- POULHZVOKOAJMA-UHFFFAOYSA-M dodecanoate Chemical compound CCCCCCCCCCCC([O-])=O POULHZVOKOAJMA-UHFFFAOYSA-M 0.000 abstract 1
- IYNRVIKPUTZSOR-HWKANZROSA-N ethenyl (e)-but-2-enoate Chemical compound C\C=C\C(=O)OC=C IYNRVIKPUTZSOR-HWKANZROSA-N 0.000 abstract 1
- FFYWKOUKJFCBAM-UHFFFAOYSA-N ethenyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC=C FFYWKOUKJFCBAM-UHFFFAOYSA-N 0.000 abstract 1
- MEGHWIAOTJPCHQ-UHFFFAOYSA-N ethenyl butanoate Chemical compound CCCC(=O)OC=C MEGHWIAOTJPCHQ-UHFFFAOYSA-N 0.000 abstract 1
- BLCTWBJQROOONQ-UHFFFAOYSA-N ethenyl prop-2-enoate Chemical compound C=COC(=O)C=C BLCTWBJQROOONQ-UHFFFAOYSA-N 0.000 abstract 1
- 150000002170 ethers Chemical class 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- XUCNUKMRBVNAPB-UHFFFAOYSA-N fluoroethene Chemical compound FC=C XUCNUKMRBVNAPB-UHFFFAOYSA-N 0.000 abstract 1
- 238000000227 grinding Methods 0.000 abstract 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-M hexanoate Chemical compound CCCCCC([O-])=O FUZZWVXGSFPDMH-UHFFFAOYSA-M 0.000 abstract 1
- 238000009775 high-speed stirring Methods 0.000 abstract 1
- 238000004898 kneading Methods 0.000 abstract 1
- 238000010030 laminating Methods 0.000 abstract 1
- 229940070765 laurate Drugs 0.000 abstract 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 abstract 1
- 125000005394 methallyl group Chemical group 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 238000003801 milling Methods 0.000 abstract 1
- 239000000178 monomer Substances 0.000 abstract 1
- 229920001220 nitrocellulos Polymers 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- HVAMZGADVCBITI-UHFFFAOYSA-M pent-4-enoate Chemical compound [O-]C(=O)CCC=C HVAMZGADVCBITI-UHFFFAOYSA-M 0.000 abstract 1
- WLJVNTCWHIRURA-UHFFFAOYSA-L pimelate(2-) Chemical compound [O-]C(=O)CCCCCC([O-])=O WLJVNTCWHIRURA-UHFFFAOYSA-L 0.000 abstract 1
- PMJHHCWVYXUKFD-UHFFFAOYSA-N piperylene Natural products CC=CC=C PMJHHCWVYXUKFD-UHFFFAOYSA-N 0.000 abstract 1
- 229920002647 polyamide Polymers 0.000 abstract 1
- 229920000728 polyester Polymers 0.000 abstract 1
- QTECDUFMBMSHKR-UHFFFAOYSA-N prop-2-enyl prop-2-enoate Chemical compound C=CCOC(=O)C=C QTECDUFMBMSHKR-UHFFFAOYSA-N 0.000 abstract 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical class CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- UBLMWQYLVOVZMT-UHFFFAOYSA-N tert-butyl n-(3-acetylphenyl)carbamate Chemical compound CC(=O)C1=CC=CC(NC(=O)OC(C)(C)C)=C1 UBLMWQYLVOVZMT-UHFFFAOYSA-N 0.000 abstract 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 abstract 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 abstract 1
- 229940070710 valerate Drugs 0.000 abstract 1
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 abstract 1
- 229940117958 vinyl acetate Drugs 0.000 abstract 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
- 239000008096 xylene Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F293/00—Macromolecular compounds obtained by polymerisation on to a macromolecule having groups capable of inducing the formation of new polymer chains bound exclusively at one or both ends of the starting macromolecule
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F291/00—Macromolecular compounds obtained by polymerising monomers on to macromolecular compounds according to more than one of the groups C08F251/00 - C08F289/00
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US286509XA | 1948-11-16 | 1948-11-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB679562A true GB679562A (en) | 1952-09-17 |
Family
ID=21844655
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB29343/49A Expired GB679562A (en) | 1948-11-16 | 1949-11-16 | Polymers and a process for the preparation thereof |
Country Status (5)
Country | Link |
---|---|
BE (1) | BE492180A (enrdf_load_stackoverflow) |
CH (1) | CH286509A (enrdf_load_stackoverflow) |
DE (1) | DE842407C (enrdf_load_stackoverflow) |
FR (1) | FR999594A (enrdf_load_stackoverflow) |
GB (1) | GB679562A (enrdf_load_stackoverflow) |
Cited By (58)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2763631A (en) * | 1952-05-23 | 1956-09-18 | Eastman Kodak Co | Acrylonitrile polymers containing vinyl chloride or vinylidene chloride |
US2779025A (en) * | 1953-08-27 | 1957-01-29 | Firestone Tire & Rubber Co | New polymeric material containing copolymerized monochlorotrifluoroethylene and an alkyl vinyl ether |
US2794793A (en) * | 1952-10-21 | 1957-06-04 | Eastman Kodak Co | Copolymerization of ethenoid monomers in the presence of polyacrylonitrile |
US2816087A (en) * | 1954-02-10 | 1957-12-10 | Eastman Kodak Co | Modified polyvinyl alcohol polymers and their preparation |
US2830032A (en) * | 1954-01-15 | 1958-04-08 | Basf Ag | Cross-linked copolymers of a polymerizable monomer with an unsaturated copolymer of a vinyl ether and vinyl allyl ether and process for making same |
US2835645A (en) * | 1955-01-05 | 1958-05-20 | Goodyear Tire & Rubber | High styrene-low diene resins of high heat softening point |
US2837496A (en) * | 1952-12-31 | 1958-06-03 | Hercules Powder Co Ltd | Graft copolymers and preparation thereof from polymer hydroperoxides |
US2838470A (en) * | 1954-02-03 | 1958-06-10 | Eastman Kodak Co | Copolymerization of acrylonitrile and another unsaturated monomer in the presence ofpreformed interpolymer |
US2842518A (en) * | 1954-09-13 | 1958-07-08 | Borg Warner | Product produced by polymerization of vinylidene chloride-acrylonitrile mixtures onto polychloroprene |
US2849419A (en) * | 1954-04-15 | 1958-08-26 | Firestone Tire & Rubber Co | Oriented filaments of graft copolymer of polyacrylate polymerized on vinylidene chloride resin |
US2858281A (en) * | 1954-01-22 | 1958-10-28 | Goodrich Co B F | Insoluble, acid and alkali-resistant carboxylic polymers |
US2859201A (en) * | 1953-11-09 | 1958-11-04 | Phillips Petroleum Co | Graft-type polymer of conjugated diene and acrylic acid and process of preparation |
US2861973A (en) * | 1956-01-31 | 1958-11-25 | Borden Co | Moldable slurry comprising vinyl butyrate and polyethyl methacrylate and molding obtained therefrom |
US2879254A (en) * | 1954-02-03 | 1959-03-24 | Eastman Kodak Co | Copolymerization of acrylonitrile and another monomer in the presence of preformed polymers and products obtained thereby |
US2883360A (en) * | 1954-02-03 | 1959-04-21 | Eastman Kodak Co | Polymerization process for preparing modified acrylonitrile polymers |
US2886551A (en) * | 1954-06-10 | 1959-05-12 | Diamond Alkali Co | Polymerization employing a phthalic glycerol alkyd resin as a suspension stabilizer |
US2886552A (en) * | 1954-06-10 | 1959-05-12 | Diamond Alkali Co | Polymerization employing polyvinyl alkyl ethers as suspension stabilizers |
US2903440A (en) * | 1958-04-08 | 1959-09-08 | Exxon Research Engineering Co | Thermo setting resin from a liquid butadiene polymer and styrene |
US2908661A (en) * | 1957-01-11 | 1959-10-13 | Borg Warner | Polymerization of acrylonitrile-alpha methyl styrene mixtures onto polybutadiene and products produced thereby |
US2941990A (en) * | 1957-07-15 | 1960-06-21 | American Cyanamid Co | Cyanoethylated polymers |
US2949437A (en) * | 1957-10-02 | 1960-08-16 | Chemstrand Corp | Composition containing blend of acrylonitrile copolymers and chlorine-containing polymer |
US2961432A (en) * | 1952-11-19 | 1960-11-22 | Basf Ag | Bulk polymerization comprising polymerizing a liquid monomer in the presence of a polymer powder |
US2961421A (en) * | 1958-02-17 | 1960-11-22 | Monsanto Chemicals | Interpolymer latices comprising acrylates and monovinylidene aromatic hydrocarbons, process of preparing same and cellulose coated therewith |
US2961423A (en) * | 1958-04-03 | 1960-11-22 | Monsanto Chemicals | Crossed-linked styrene-allyl alcohol copolymers as binders for fibrous fillers and structural units manufactured therefrom |
US2963453A (en) * | 1957-03-15 | 1960-12-06 | Rohm & Haas | Acrylic and methacrylic acid resins controllably crosslinked with polyallyl acrylate, its substituted derivatives, and copolymers thereof |
US2981650A (en) * | 1955-02-25 | 1961-04-25 | Degussa | Adhesives, cements and the like |
US2992203A (en) * | 1957-03-25 | 1961-07-11 | Rohm & Haas | High impact resistant polymers derived primarily from esters of acrylic and methacrylic acids |
US3019208A (en) * | 1954-01-18 | 1962-01-30 | Firestone Tire & Rubber Co | Method of making graft copolymers of vinyl chloride and polyacrylate |
US3020257A (en) * | 1958-02-12 | 1962-02-06 | Haris Co Ltd | Method for manufacture of polyisobutylene-vinyl acetate graft copolymer |
DE1123476B (de) * | 1953-09-08 | 1962-02-08 | Phil Oliver Wallis Burke Jun D | Verfahren zur Herstellung von unloeslichen, vernetzten Hochpolymeren kolloider Teilchengroesse |
US3041309A (en) * | 1959-04-24 | 1962-06-26 | Monsanto Chemicals | Blend of styrene copolymer with a graft-copolymer of an alkyl methacrylate upon an alkyl acrylate polymer |
US3055859A (en) * | 1956-09-28 | 1962-09-25 | Basf Ag | Impact-resistant plastic compositions comprising a styrene polymer and a cross-linked acrylic acid ester polymer, and process for preparing same |
US3061582A (en) * | 1959-07-09 | 1962-10-30 | Nat Distillers Chem Corp | Ethylenic modification of branched chain polyamides |
US3061581A (en) * | 1959-07-09 | 1962-10-30 | Nat Distillers Chem Corp | Vinyl modification of branched chain polyamides |
US3062777A (en) * | 1953-04-14 | 1962-11-06 | Union Carbide Corp | Graft copolymers of styrene on butadiene rubbers and method for making same |
US3074866A (en) * | 1958-01-06 | 1963-01-22 | Alelio Gaetano F D | Irradiated polymers |
US3075905A (en) * | 1958-01-06 | 1963-01-29 | Alelio Gaetano F D | Irradiated polymers |
US3075904A (en) * | 1958-01-06 | 1963-01-29 | Alelio Gaetano F D | Irradiated polymers |
US3081168A (en) * | 1954-03-26 | 1963-03-12 | Time Inc | Polyamide photographic printing plate and method of using same |
US3082161A (en) * | 1958-01-06 | 1963-03-19 | Alelio Gaetano F D | Irradiated polymers |
US3091595A (en) * | 1956-03-22 | 1963-05-28 | Shell Oil Co | Cyano-substituted polyamides and their use as curing agents for polyepoxides |
US3092512A (en) * | 1957-10-31 | 1963-06-04 | Table ii | |
US3099631A (en) * | 1958-03-06 | 1963-07-30 | Du Pont | Nitrogenous condensation polymer containing grafted acid |
US3113912A (en) * | 1959-07-16 | 1963-12-10 | Phillips Petroleum Co | Preparation of vulcanizates by irradiation of block copolymers |
US3128528A (en) * | 1960-04-28 | 1964-04-14 | Du Pont | Preparation of hydroset textile material |
US3135717A (en) * | 1960-02-10 | 1964-06-02 | Grace W R & Co | Process of forming graft copolymers of polystyrene and polyvinyl chloride |
US3177270A (en) * | 1960-10-10 | 1965-04-06 | Dow Chemical Co | Graft copolymers of polyolefins and monovinyl aromatic compounds and method of making the same |
US3177269A (en) * | 1960-10-10 | 1965-04-06 | Dow Chemical Co | Graft copolymers of polyolefins and acrylic and methacrylic acid and method of making the same |
US3188228A (en) * | 1958-05-14 | 1965-06-08 | Du Pont | Method of graft polymerizing an organic compound to a solid shaped condensation polymer structure |
US3261885A (en) * | 1960-10-07 | 1966-07-19 | Roemmler Gmbh H | Production of block-graft copolymers from polyolefines and synthetic polyamides |
US3261887A (en) * | 1958-02-14 | 1966-07-19 | Us Rubber Co | Transparent gum plastic composition containing methyl methacrylate resin and graft copolymer |
US3294711A (en) * | 1963-04-22 | 1966-12-27 | Bayer Ag | Graft polymers of vinyl acetate or vinyl chloride onto a saturated polyester backbone, and polyurethane foams therefrom |
US3296339A (en) * | 1966-01-20 | 1967-01-03 | Rohm & Haas | Thermoplastic compositions formed by polymerizing methacrylic acid esters and polybutadiene latices |
US3297471A (en) * | 1965-04-08 | 1967-01-10 | Du Pont | Acrylic or methacrylic acid grafting copolymerized on nylon and forming salt of said graft |
US3413378A (en) * | 1966-11-14 | 1968-11-26 | Du Pont | Graft copolymers of nitrile groups on polyamide substrates |
EP0344699A3 (en) * | 1988-06-02 | 1991-03-27 | Bromine Compounds Ltd. | Process for the polymerization of pentabromobenzylester monoacrylate |
US6228948B1 (en) | 1998-01-16 | 2001-05-08 | E. I. Du Pont De Nemours And Company | High melt flow, highly-grafted polypropylene |
DE102007011825B3 (de) * | 2007-03-12 | 2008-05-15 | Deutsche Gumtec Ag | Verfahren zur Modifizierung von Gummi- und Thermoplastabfällen mittels Pfropfung während eines Mahlprozesses sowie Verwendung der so modifizierten Gummi-und Thermoplastabfälle |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2899405A (en) * | 1959-08-11 | Polymerization of vinyl chloride or | ||
US2741650A (en) * | 1951-11-08 | 1956-04-10 | Shawinigan Resins Corp | Styrene-modified polyvinyl acetate resins |
US2719136A (en) * | 1951-11-29 | 1955-09-27 | Eastman Kodak Co | Compositions from polymerizing acrylonitrile in the presence of maleic anhydride copolymers |
US2773050A (en) * | 1952-04-30 | 1956-12-04 | Eastman Kodak Co | Water vapor permeable compositions and articles containing a polyacrylic ester and polyvinyl alcohol |
US2879253A (en) * | 1954-02-03 | 1959-03-24 | Eastman Kodak Co | Copolymerization of acrylonitrile and another unsaturated monomer, in the presence of preformed homopolymers and products obtained thereby |
US2713568A (en) * | 1953-03-04 | 1955-07-19 | Firestone Tire & Rubber Co | Stripping vinylidene-vinyl chloride copolymers with aid of alkyl acrylate and product |
US2784172A (en) * | 1953-04-27 | 1957-03-05 | Monsanto Chemicals | Acrylonitrile copolymers stabilized with acrylic acid salts |
US2879256A (en) * | 1954-11-26 | 1959-03-24 | Eastman Kodak Co | Continuous process for preparing vinyl or vinylidene chloride graft polymers of improved solubility |
DE1012071B (de) * | 1955-02-22 | 1957-07-11 | Courtaulds Ltd | Verfahren zur Herstellung von Blockmischpolymeren |
NL104706C (enrdf_load_stackoverflow) * | 1955-12-09 | 1963-05-15 | ||
US2991269A (en) * | 1956-02-21 | 1961-07-04 | Shell Oil Co | Process for preparing block copolymers by degrading a preformed polymer in the presence of dissimilar monomer |
US2905653A (en) * | 1957-05-14 | 1959-09-22 | Firestone Tire & Rubber Co | Oriented products from graft copolymers of vinyl ester on acrylonitrile polymer |
NL301879A (enrdf_load_stackoverflow) * | 1962-12-26 |
-
0
- BE BE492180D patent/BE492180A/xx unknown
-
1949
- 1949-11-04 DE DEN124A patent/DE842407C/de not_active Expired
- 1949-11-15 CH CH286509D patent/CH286509A/de unknown
- 1949-11-15 FR FR999594D patent/FR999594A/fr not_active Expired
- 1949-11-16 GB GB29343/49A patent/GB679562A/en not_active Expired
Cited By (60)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2763631A (en) * | 1952-05-23 | 1956-09-18 | Eastman Kodak Co | Acrylonitrile polymers containing vinyl chloride or vinylidene chloride |
US2794793A (en) * | 1952-10-21 | 1957-06-04 | Eastman Kodak Co | Copolymerization of ethenoid monomers in the presence of polyacrylonitrile |
US2961432A (en) * | 1952-11-19 | 1960-11-22 | Basf Ag | Bulk polymerization comprising polymerizing a liquid monomer in the presence of a polymer powder |
US2837496A (en) * | 1952-12-31 | 1958-06-03 | Hercules Powder Co Ltd | Graft copolymers and preparation thereof from polymer hydroperoxides |
US3062777A (en) * | 1953-04-14 | 1962-11-06 | Union Carbide Corp | Graft copolymers of styrene on butadiene rubbers and method for making same |
US2779025A (en) * | 1953-08-27 | 1957-01-29 | Firestone Tire & Rubber Co | New polymeric material containing copolymerized monochlorotrifluoroethylene and an alkyl vinyl ether |
DE1123476B (de) * | 1953-09-08 | 1962-02-08 | Phil Oliver Wallis Burke Jun D | Verfahren zur Herstellung von unloeslichen, vernetzten Hochpolymeren kolloider Teilchengroesse |
US2859201A (en) * | 1953-11-09 | 1958-11-04 | Phillips Petroleum Co | Graft-type polymer of conjugated diene and acrylic acid and process of preparation |
US2830032A (en) * | 1954-01-15 | 1958-04-08 | Basf Ag | Cross-linked copolymers of a polymerizable monomer with an unsaturated copolymer of a vinyl ether and vinyl allyl ether and process for making same |
US3019208A (en) * | 1954-01-18 | 1962-01-30 | Firestone Tire & Rubber Co | Method of making graft copolymers of vinyl chloride and polyacrylate |
US2858281A (en) * | 1954-01-22 | 1958-10-28 | Goodrich Co B F | Insoluble, acid and alkali-resistant carboxylic polymers |
US2879254A (en) * | 1954-02-03 | 1959-03-24 | Eastman Kodak Co | Copolymerization of acrylonitrile and another monomer in the presence of preformed polymers and products obtained thereby |
US2883360A (en) * | 1954-02-03 | 1959-04-21 | Eastman Kodak Co | Polymerization process for preparing modified acrylonitrile polymers |
US2838470A (en) * | 1954-02-03 | 1958-06-10 | Eastman Kodak Co | Copolymerization of acrylonitrile and another unsaturated monomer in the presence ofpreformed interpolymer |
US2816087A (en) * | 1954-02-10 | 1957-12-10 | Eastman Kodak Co | Modified polyvinyl alcohol polymers and their preparation |
US3081168A (en) * | 1954-03-26 | 1963-03-12 | Time Inc | Polyamide photographic printing plate and method of using same |
US2849419A (en) * | 1954-04-15 | 1958-08-26 | Firestone Tire & Rubber Co | Oriented filaments of graft copolymer of polyacrylate polymerized on vinylidene chloride resin |
US2886551A (en) * | 1954-06-10 | 1959-05-12 | Diamond Alkali Co | Polymerization employing a phthalic glycerol alkyd resin as a suspension stabilizer |
US2886552A (en) * | 1954-06-10 | 1959-05-12 | Diamond Alkali Co | Polymerization employing polyvinyl alkyl ethers as suspension stabilizers |
US2842518A (en) * | 1954-09-13 | 1958-07-08 | Borg Warner | Product produced by polymerization of vinylidene chloride-acrylonitrile mixtures onto polychloroprene |
US2835645A (en) * | 1955-01-05 | 1958-05-20 | Goodyear Tire & Rubber | High styrene-low diene resins of high heat softening point |
US2981650A (en) * | 1955-02-25 | 1961-04-25 | Degussa | Adhesives, cements and the like |
US2861973A (en) * | 1956-01-31 | 1958-11-25 | Borden Co | Moldable slurry comprising vinyl butyrate and polyethyl methacrylate and molding obtained therefrom |
US3091595A (en) * | 1956-03-22 | 1963-05-28 | Shell Oil Co | Cyano-substituted polyamides and their use as curing agents for polyepoxides |
US3055859A (en) * | 1956-09-28 | 1962-09-25 | Basf Ag | Impact-resistant plastic compositions comprising a styrene polymer and a cross-linked acrylic acid ester polymer, and process for preparing same |
US2908661A (en) * | 1957-01-11 | 1959-10-13 | Borg Warner | Polymerization of acrylonitrile-alpha methyl styrene mixtures onto polybutadiene and products produced thereby |
US2963453A (en) * | 1957-03-15 | 1960-12-06 | Rohm & Haas | Acrylic and methacrylic acid resins controllably crosslinked with polyallyl acrylate, its substituted derivatives, and copolymers thereof |
US2992203A (en) * | 1957-03-25 | 1961-07-11 | Rohm & Haas | High impact resistant polymers derived primarily from esters of acrylic and methacrylic acids |
US2941990A (en) * | 1957-07-15 | 1960-06-21 | American Cyanamid Co | Cyanoethylated polymers |
US2949437A (en) * | 1957-10-02 | 1960-08-16 | Chemstrand Corp | Composition containing blend of acrylonitrile copolymers and chlorine-containing polymer |
US3092512A (en) * | 1957-10-31 | 1963-06-04 | Table ii | |
US3074866A (en) * | 1958-01-06 | 1963-01-22 | Alelio Gaetano F D | Irradiated polymers |
US3075905A (en) * | 1958-01-06 | 1963-01-29 | Alelio Gaetano F D | Irradiated polymers |
US3075904A (en) * | 1958-01-06 | 1963-01-29 | Alelio Gaetano F D | Irradiated polymers |
US3082161A (en) * | 1958-01-06 | 1963-03-19 | Alelio Gaetano F D | Irradiated polymers |
US3020257A (en) * | 1958-02-12 | 1962-02-06 | Haris Co Ltd | Method for manufacture of polyisobutylene-vinyl acetate graft copolymer |
US3261887A (en) * | 1958-02-14 | 1966-07-19 | Us Rubber Co | Transparent gum plastic composition containing methyl methacrylate resin and graft copolymer |
US2961421A (en) * | 1958-02-17 | 1960-11-22 | Monsanto Chemicals | Interpolymer latices comprising acrylates and monovinylidene aromatic hydrocarbons, process of preparing same and cellulose coated therewith |
US3099631A (en) * | 1958-03-06 | 1963-07-30 | Du Pont | Nitrogenous condensation polymer containing grafted acid |
US2961423A (en) * | 1958-04-03 | 1960-11-22 | Monsanto Chemicals | Crossed-linked styrene-allyl alcohol copolymers as binders for fibrous fillers and structural units manufactured therefrom |
US2903440A (en) * | 1958-04-08 | 1959-09-08 | Exxon Research Engineering Co | Thermo setting resin from a liquid butadiene polymer and styrene |
US3188228A (en) * | 1958-05-14 | 1965-06-08 | Du Pont | Method of graft polymerizing an organic compound to a solid shaped condensation polymer structure |
US3041309A (en) * | 1959-04-24 | 1962-06-26 | Monsanto Chemicals | Blend of styrene copolymer with a graft-copolymer of an alkyl methacrylate upon an alkyl acrylate polymer |
US3041308A (en) * | 1959-04-24 | 1962-06-26 | Monsanto Chemicals | Blend of styrene copolymer with a graft-copolymer of styrene and an alkyl methacrylate upon an alkyl acrylate polymer |
US3041306A (en) * | 1959-04-24 | 1962-06-26 | Monsanto Chemicals | Blend of a styrene copolymer with a graft-copolymer of styrene upon an alkyl acrylate polymer |
US3061582A (en) * | 1959-07-09 | 1962-10-30 | Nat Distillers Chem Corp | Ethylenic modification of branched chain polyamides |
US3061581A (en) * | 1959-07-09 | 1962-10-30 | Nat Distillers Chem Corp | Vinyl modification of branched chain polyamides |
US3113912A (en) * | 1959-07-16 | 1963-12-10 | Phillips Petroleum Co | Preparation of vulcanizates by irradiation of block copolymers |
US3135717A (en) * | 1960-02-10 | 1964-06-02 | Grace W R & Co | Process of forming graft copolymers of polystyrene and polyvinyl chloride |
US3128528A (en) * | 1960-04-28 | 1964-04-14 | Du Pont | Preparation of hydroset textile material |
US3261885A (en) * | 1960-10-07 | 1966-07-19 | Roemmler Gmbh H | Production of block-graft copolymers from polyolefines and synthetic polyamides |
US3177269A (en) * | 1960-10-10 | 1965-04-06 | Dow Chemical Co | Graft copolymers of polyolefins and acrylic and methacrylic acid and method of making the same |
US3177270A (en) * | 1960-10-10 | 1965-04-06 | Dow Chemical Co | Graft copolymers of polyolefins and monovinyl aromatic compounds and method of making the same |
US3294711A (en) * | 1963-04-22 | 1966-12-27 | Bayer Ag | Graft polymers of vinyl acetate or vinyl chloride onto a saturated polyester backbone, and polyurethane foams therefrom |
US3297471A (en) * | 1965-04-08 | 1967-01-10 | Du Pont | Acrylic or methacrylic acid grafting copolymerized on nylon and forming salt of said graft |
US3296339A (en) * | 1966-01-20 | 1967-01-03 | Rohm & Haas | Thermoplastic compositions formed by polymerizing methacrylic acid esters and polybutadiene latices |
US3413378A (en) * | 1966-11-14 | 1968-11-26 | Du Pont | Graft copolymers of nitrile groups on polyamide substrates |
EP0344699A3 (en) * | 1988-06-02 | 1991-03-27 | Bromine Compounds Ltd. | Process for the polymerization of pentabromobenzylester monoacrylate |
US6228948B1 (en) | 1998-01-16 | 2001-05-08 | E. I. Du Pont De Nemours And Company | High melt flow, highly-grafted polypropylene |
DE102007011825B3 (de) * | 2007-03-12 | 2008-05-15 | Deutsche Gumtec Ag | Verfahren zur Modifizierung von Gummi- und Thermoplastabfällen mittels Pfropfung während eines Mahlprozesses sowie Verwendung der so modifizierten Gummi-und Thermoplastabfälle |
Also Published As
Publication number | Publication date |
---|---|
CH286509A (de) | 1952-10-31 |
DE842407C (de) | 1952-06-26 |
FR999594A (fr) | 1952-02-01 |
BE492180A (enrdf_load_stackoverflow) |
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